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Cat. No. Product Name Information
PC-28360

XJB-5-131

Antioxidant

XJB-5-131 is hemigramicidin-TEMPO conjugate and mitochondria-targeted ROS and electron scavenger, reduces apoptosis and enhances cell survival in mouse embryonic cells in vitro, improves mitochondrial function.
PC-28349

Herbacetin

Ornithine decarboxylase inhibitor

Herbacetin is a naturally occurring flavonoid and potent, specific, allosteric ornithine decarboxylase (ODC) inhibitor, exhibits potent anticancer activity in colon cancer cell lines expressing high levels of ODC.
PC-28332

PANK-IN-3

PANK3 inhibitor

PANK-IN-3 is a high-affinity, selective inhibitor of PANK3 (Pantothenate kinase 3) with Ki of 4.2 nM, 104-fold selective over PanK1β.
PC-28331

PANK-IN-2

PANK inhibitor

PANK-IN-2 is a poten tinhibitor of Pantothenate kinase (PANK) with IC50 of 92 nM for PanK2, 70 nM for PanK1β, and 25 nM for PanK3 respectively in radiochemical enzyme assays.
PC-28330

PANK-IN-1

PANK3 inhibitor

PANK-IN-1 is a potent, pantothenate competitive inhibitor of Pantothenate kinase (PANK) with IC50 of 0.51 uM against PANK3.
PC-28291

Racemetirosine

Tyrosine hydroxylase inhibitor

Racemetirosine (Alpha-methyltyrosine, alphaMT, Alpha-methyl-para-tyrosine) is a competitive small molecule tyrosine hydroxylase inhibitor, inhibits catecholamine biosynthesis, blocks hydroxylation of tyrosine into dihydroxyphenylalanine (DOPA).
PC-28249

SARM1 inhibitor B339

SARM1 inhibitor

SARM1 inhibitor B339 is a potent SARM1 inhibitor with IC50 of 7.215 uM, shows potential in prevention of axonal degeneration.
PC-28230

NSC 65828 sodium

Angiogenin inhibitor

NSC 65828 sodium (NCI-65828) is a small-molecule inhibitor of the ribonucleolytic activity of human angiogenin with Ki of 81 uM; possess antitumor activity in mice.
PC-28145

FM029

FOXP3-T-bet stabliezer

FM029 is a direct FOXP3 targeting small molecule that binds to FOXP3 (SPR KD=1.13 uM), stabilizes the FOXP3-T-bet interaction to represses T-bet-driven IFN-γ production.
PC-28105

SEP-227900

DAAO inhibitor

SEP-227900 is an orally active small molecule D-amino-acid oxidase (DAAO) inhibitor.
PC-28104

AS057278

DAAO inhibitor

AS057278 (MPCA, U-19425) is a potent, selective, orally active and blood-brain barrier (BBB) penetrant D-amino acid oxidase (DAAO) inhibitor with IC50 of 0.91 uM, shows potential anti-psychotic properties, also inhibits adipocyte lipolysis.
PC-28054

MOG (35-55) mouse, rat

MOG peptide

MOG (35-55) mouse, rat is a myelin oligodendrocyte glycoprotein (MOG) peptide derived from the extracellular domain of MOG protein and key immunodominant epitope extensively utilized in the study of autoimmune demyelinating diseases of the central nervous system (CNS), induce experimental autoimmune encephalomyelitis (EAE) in susceptible animal models, particularly C57BL/6 mice.

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